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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 339915Generated: October 31, 2026

Acetyl chloride → HCID 178466087, compound

https://huagongshe.com/reaction/339915

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantPotassium AcetateHCID 517044—
ReactantHCID 178419233HCID 178419233—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 178466087HCID 17846608741.9%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a suspension of [5-(4-boroxyphenyl)-6,6-dimethyl-4,4-dioxo-5,6-dihydro-4H-4lambda*6*-[1,4,3]oxathiazin-2-yl]-[(S)-3-(tert-butyldimethylsilanyloxy)-1-(2-fluorophenyl)propyl]amine (400 mg) and potassium acetate (140 mg) in dioxane (6 ml) were added bis(triphenylphosphine)palladium(II)dichloride (60 mg) and acetyl chloride (120 μl), and the mixture was stirred at 50° C. overnight. The mixture was diluted with ethyl acetate, washed with water, dried over magnesium sulfate and concentrated. This was followed by purification by column chromatography (ethyl acetate/heptane). This gave the product (172 mg) with a molecular weight of 562.8 g/mol (C28H39FN2O5SSi).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895547B2
Source datasetuspto-grants-2014_11
ORD IDord-3bdde6afe268461dbd7b8a7b58c9aa19
Source noteuspto-grants-2014_11